drugset / Trial / NCT01892384
Safety and Tolerability of BI 409306 in Patients With Schizophrenia
RandomizedParallel-groupDouble-blindTreatment
Summary
The primary objective of the current study is to investigate the safety and tolerability of BI 409306 in schizophrenic patients following oral administration of multiple low, medium, and high doses over 14 days. A secondary objective is the exploration of the pharmacokinetics and pharmacodynamics of BI 409306 in schizophrenic patients.
Timeline
- Start
- 2013-06-28
- Primary completion
- 2013-12-05
- Completion
- 2013-12-05
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | OSORESNONTRINE | Small molecule | 25 mg | Oral |
| Subject | OSORESNONTRINE | Small molecule | 50 mg | Oral |
| Subject | OSORESNONTRINE | Small molecule | 100 mg | Oral |